Complexes of the formula ##STR1## wherein R1 is hydrocarbyl or substituted hydrocarbyl, EACH OF R2 and R3 is independently hydrogen, lower alkyl or substituted lower alkyl,
Each of X1 and X2 is independently halo, nitro, alkyl, substituted alkyl, alkoxy or substituted alkoxy,
M+ is a cation, e.g., lithium, sodium, potassium or ammonium, and
m is 0 or 1,
n is 0 or 1, and
p is 0 or 1,
With the proviso that the sum of m, n and p is 1, and derivatives thereof wherein Ring A is substituted. These complexes are good dyes for nautral and synthetic polyamide fibers (e.g., wool, silk and Nylon) as well as for leather and light metals (e.g., aluminum)... The shades of the dyeings range from olive to yellowish-green to khaki-brown. The dyeings have notable fastness to light, wet treatments, rubbing and pressing and stability to alkalis and acids and satisfactory dischargeability. The dyes build-up on polyamides from neutral medium.
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1. A complex of the formula ##STR6## wherein R1 is alkyl of 1 to 12 carbon atoms, substituted alkyl wherein the alkyl chain has 1 to 12 carbon atoms and each substituent is independently halo, cyano or lower alkoxy, cyclohexyl, phenyl or substituted phenyl wherein each substituent is independently halo, lower alkyl, lower alkoxy, cyano, carboxy or lower alkoxy carbonyl,
each of R2 and R3 is independently hydrogen, lower alkyl or substituted lower alkyl wherein each substituent is independently halo, hydroxy or lower alkoxy, each of X1 and X2 is independently halo, nitro, trifluoromethyl, alkyl of 1 to 6 carbon atoms, substituted alkyl, alkoxy of 1 to 6 carbon atoms or substituted alkoxy, wherein each alkyl chain of substituted alkyl and alkoxy chain of substituted alkoxy independently has 1 to 6 carbon atoms and each substituent is independently halo, trifluoromethyl or cyano, M30 is lithium, sodium, potassium or ammonium, m is 0 or 1, n is 0 or 1, and p is 0 or 1,
with the proviso that the sum of m, n and p is 1, wherein each halo is independently chloro or bromo. 2. A complex according to
wherein R1 is alkyl of 1 to 12 carbon atoms, alkyl of 1 to 12 carbon atoms substituted by halo, lower alkoxy or cyano, cyclohexyl, phenyl or phenyl substituted by halo, lower alkyl, lower alkoxy, cyano, carboxy or lower alkoxycarbonyl, each of R2 and R3 is independently hydrogen, lower alkyl or lower alkyl substituted by halo, hydroxy or lower alkoxy, and each of X1 and X2 is independently halo, nitro, trifluoromethyl, alkyl of 1 to 6 carbon atoms, alkyl of 1 to 6 carbon atoms substituted by halo, trifluoromethyl or cyano, alkoxy of 1 to 6 carbon atoms or alkoxy of 1 to 6 carbon atoms substituted by halo, trifluoromethyl or cyano,
wherein each halo is independently chloro or bromo. 3. A complex according to
R2 is hydrogen, alkyl of 1 to 4 carbon atoms or alkyl of 1 to 4 carbon atoms substituted by hydroxy or lower alkoxy, X1 is nitro, halo or lower alkoxy, X2 is nitro or halo, M30 is lithium, sodium, potassium or ammonium, m is 0 or 1, n is 0 or 1, and p is 0 or 1,
With the provisos that a. the SO2 NH-R2 group is para to the oxygen atom or para to the azo group attached to the benzene ring to which it is attached, b. the X2 substituent is meta or para to the azo group attached to the benzene ring to which it is attached, and c. the sum of m, n and p is 1. 6. A complex according to
each of R2 and R3 is independently hydrogen or alkyl of 1 to 4 carbon atoms, each of X1 and X2 is independently halo or nitro, M30 is lithium, sodium, potassium or ammonium, m is 0 or 1, n is 0 or 1, p is 0 or 1,
with the proviso that the sum of m, n and p is 1, wherein each halo is independently chloro or bromo. 7. A complex according to
each of R2 and R3 is independently hydrogen or alkyl of 1 to 4 carbon atoms, each of X1 and X2 is independently nitro or halo, and M30 is lithium, sodium, potassium or ammonium.
8. A complex according to
9. A complex according to
each of X1 and X2 is independently nitro, chloro or bromo, and M30 is lithium, sodium, potassium or ammonium, with the provisos that a. one of X1 and X2 is ortho to the oxygen atom and the other is para to the oxygen atom attached to the benzene ring to which they are attached, b. the -SO2 NH2 group is para to the oxygen atom or para to the azo group attached to the benzene ring to which it is attached, and c. the SO3 H group is ortho or para to the nitrogen atom attached to the benzene ring to which it is attached.
10. A complex according to
11. A complex according to
M30 is lithium, sodium, potassium or ammonium, with the proviso that the SO3 H group is ortho or para to the nitrogen atom attached to the benzene ring to which it is attached.
17. A composition of matter consisting essentially of a complex according to
each of R2 and R3 is independently hydrogen or alkyl of 1 to 4 carbon atoms, each of X1 and X2 is independently nitro or halo, and M+ is lithium, sodium, potassium or ammonium.
18. As a composition of matter, an asymmetrical 1:2 cobalt complex according to
19. A complex according to
wherein R1 is alkyl of 1 to 12 carbon atoms, cyclohexyl, phenyl or substituted phenyl each substituent of which is independently halo, lower alkyl or lower alkoxy, each of X1 and X2 is independently halo, nitro, alkyl of 1 to 6 carbon atoms or alkoxy of 1 to 6 carbon atoms, and each of R1 and R2 is independently hydrogen, lower alkyl or lower alkyl substituted by halo, hydroxy or lower alkoxy. 20. A composition of matter consisting essentially of a complex according to
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This application is a continuation-in-part of application Ser. No. 189,768, filed Oct. 15, 1971 and now abandoned.
This invention relates to new 2:1 cobalt complexes of a 1:1 cobalt complex of an aminophenol→2-phenylaminonaphthalene sulfonic acid azo dye and an aminophenolsulfonamide→Acetoacetylphenylamideazo dye.
More particularly the new dyes correspond to the formula ##STR2## where
R1 stands for a hydrocarbon radical which may be substituted,
R2 and R3 each stands for hydrogen or a lower alkyl radical which may be substituted,
X1 and X2 each stands for halogen, a nitro group or an alkyl or alkoxy radical which may be substituted,
M+ for a cation, and the ring A may be further substituted.
The aforestated cobalt complex compounds can be produced by reacting a 1:1 cobalt complex of a monoazo compound of the formula ##STR3## where X1 and X2 have one of the aforestated meanings, with a monoazo compound of the formula ##STR4## where R1, R2 and R3 likewise have the aforestated meanings.
Alkyl, cycloalkyl and aryl radicals are suitable for substituents R1. The alkyl radicals contain preferably 1 to 12 carbon atoms, may be straight or branched and may bear further substituents such as halogen atoms, alkoxy groups, cyano groups and the like. The first choice as aryl radicals are phenyl radicals which also may be substituted by halogen atoms such as chlorine or bromine, alkyl or alkoxy radicals, a cyano group, the carboxy group, an alkoxycarbonyl group and the like.
The radicals R2 and R3 may be hydrogen or lower alkyl radicals which may be straight or branched and may bear further substituents such as halogen atoms or hydroxy or lower alkoxy groups.
If X1 and X2 represent halogen, chlorine and bromine are the preferred meanings. The trifluoromethyl group also is a preferred substituent. The alkyl or alkoxy radicals, which may be substituted, are preferably lower radicals having 1 to 6 carbon atoms and if they are substituted they bear substituents such as halogen, primarily chlorine or bromine, the trifluoromethyl group or cyano radicals. It is preferable for one or both the radicals X1 and X2 to be nitro groups.
The cation M30 is preferably a lithium, sodium, potassium or ammonium cation.
The preferred 2:1 cobalt complex compounds of the general formula (I) above are those in which the radical R1 is a straight or branched alkyl radical having 4 to 12 carbon atoms, a phenyl radical or a cycloalkyl radical, R2 and R3 are hydrogen or lower alkyl radicals with 1 to 4 carbon atoms, X1 and X2 are nitro groups or halogen atoms, and where the SO3 H group occurs in the ring A and this ring is not substituted further.
More specially preferred 2:1 cobalt complex compounds of the present invention are those in which the radical R1 is a branched alkyl radical with 6 to 10 carbon atoms or a phenyl radical, R2 and R3 are hydrogen, X1 and X2 are nitro groups, chlorine or bromine atoms in the 4- and 6-positions to the oxygen group on the benzene radical, the SO2 -NR2 R3 group (preferably SO2 NH2 group) occupies the 4- or 5-position to the oxygen group on the benzene radical and the SO3 H group in the ring A of formula (I) is in the 2- or 4-position to the amino group. The 2:1 cobalt complex compounds disclosed herein are best produced in aqueous or aqueous-organic solutions. The starting 1:1 cobalt complexes, which in part are known and whose formation is described below, are reacted preferably with stoichiometric amounts of the metal-free monoazo dye. The reaction takes place in alkaline solution and is allowed to proceed until the entire amount of the 1:1 cobalt complex has reacted. The 2:1 cobalt complex formed is then salted out, washed with a concentrated salt solution, collected and dried. The 2:1 cobalt complexes produced in accordance with this invention are readily soluble in water.
Some 1:1 cobalt complexes required as starting materials are known and are described in the literature, for example in French Pat. Nos. 1,431,264, 1,466,877 and 1,476,587.
The preferred starting material is a 1:1 cobalt complex which can be produced as follows. An azo dye of formula (II) is reacted with an agent donating cobalt in the presence of a nitrite, either in water, in a mixture of water and an organic solvent or in an organic solvent alone. The suitable temperature range for the reaction is about 0° to 60° C, the optimum range being 10°-30° C, and the reaction medium is set in the acid region, i.e. at a pH from 3 to 7 or preferably pH 5 to 6.
Cobalt donating compounds particularly suitable for the reaction include cobaltous formate, acetate, nitrate and sulphate. For formation of the 2:1 cobalt complex compounds it is best to employ 3-6 mols of the nitrite per gram atom of cobalt. In comparison with the known methods of cobalt complex formation the new process disclosed herein has the advantage that the 1:1 cobalt complex compounds are obtained in much greater purity and homogeneity; they are in fact quite free from by-products. It has been found that by using these highly pure 1:1 cobalt complexes, substantially pure asymmetrical 2:1 complexes are obtained (at least 95% pure).
The monoazo compounds of formula (III) employed as second starting material are for the most part known or can be produced by known methods. Their production is described, for example, in French Pat. Nos. 1,107,888 and 1,061,329.
As is evident to those in the art, the sulpho group of the complexes is usually in salt form, e.g. alkali metal salts.
The new 2:1 cobalt complex compounds obtained in accordance with this invention are useful for the dyeing of natural and synthetic polyamide fibers, e.g. wool, silk and nylon, and for the dyeing of leather and metals, notably aluminum.
The dyes disclosed herein give dyeings which have notable fastness to light and wet treatments (water, sea water, milling and perspiration) with notable rubbing fastness. The dyes build up on polyamide fibres from neutral medium and as they are of asymmetrical nature, they show the desired property of a uniform rate of dyeing, in contrast to the compounds described in Swiss Patent 317,120. Furthermore, the dyeings obtained have notable wash fastness, hot water fastness, pressing fastness, are stable to alkali and acids and have satisfactory dischargeability. The dyeings made on wool exhibit notable carbonization fastness.
In the following Examples the parts are by weight and the temperatures in degrees centigrade.
The 1:1 cobalt complex from 51 parts of the monoazo dye 2-amino-1-hydroxy-4, 6-dinitrobenzene-2-phenylaminonaphthalene-4'-sulphoni c acid, whose method of production is described below, and 41 parts of the dye formed by coupling diazotized 2-amino-1-hydroxybenzene-4-sulphonic acid amide to 1-acetoacetylamino-2-ethylhexane are stirred into 500 parts of water and 150 parts of alcohol, then dissolved by the addition of sodium hydroxide solution at pH 12.0 and 20°. Stirring is continued for a few hours at 20° until the 1:1 cobalt complex has completely disappeared. The solution is filtered and potassium chloride is added to salt out the dye. It is filtered, washed with 20% potassium chloride solution and dried. The dye obtained, which is at least 95% pure, has the formula ##STR5## and dissolves readily in water and dyes natural and synthetic polyamide fibres in olive green shades.
The dyeings show notable fastness to light, rubbing and wet treatments such as water, sea water, milling and perspiration.
The 1:1 cobalt complex used as starting material in the above procedure is produced as follows.
A solution of 28 parts of cobaltous sulphate × 7H2 O and 42 parts of sodium nitrite in 400 parts of water is prepared. At 10° 51 parts of the dye obtained by acid coupling of diazotized 2-amino-1-hydroxy-4,6-dinitrobenzene to 2-phenylaminonaphthalene-4'-sulphonic acid are added, whereupon the dye goes partly into solution. To complete dissolution, 50 parts of dimethylformamide are added dropwise. The pH is maintained at 5.0-5.5 by adding hydrochloric acid. The metallising reaction commences at once and after approximately 2 hours is complete. Salt is added to precipitate the 1:1 cobalt complex and it is isolated by filtration, washed with water and dried.
The 1:1 cobalt complexes used as starting materials in Examples II to XIII are produced in an analogous manner.
The following dyes can be produced in the same manner.
| Examples II - XIII |
| ______________________________________ |
| Color |
| of the |
| 1:2- |
| 1:1 Co-Complex Com- |
| of the dye reacted with plexes |
| ______________________________________ |
| II 2-amino-1-hydroxy- |
| 2-amino-1-hydroxy- |
| olive |
| 4,6-dinitrobenzene→ |
| benzene-4-sulphonic |
| 2-phenylaminonaph- |
| acid-amide→acetoace- |
| thalene-4'-sulphonic |
| tylaminobenzene |
| acid |
| III 2-amino-1-hydroxy- |
| " olive |
| 4,6-dinitrobenzene→ |
| 2-phenylaminonaph- |
| thalene-2'-sulphonic |
| acid |
| IV " 2-amino-1-hydroxy- |
| yellow- |
| benzene-4-sulphonic |
| ish |
| acid-amide→1-aceto- |
| green |
| acetylamino-2-ethyl- |
| hexane |
| V 2-amino-1-hydroxy- |
| 2-amino-1-hydroxy- |
| olive |
| 4,6-dinitrobenzene→ |
| benzene-5-sulphonic |
| 2-phenylaminonaph- |
| acid-methylamide→1- |
| thalene-6-sulphonic |
| acetoacetylamino-2- |
| acid ethylhexane |
| VI 2-amino-1-hydroxy- |
| 2-amino-1-hydroxy- |
| Khaki |
| 4,6-dinitrobenzene→ |
| benzene-4-sulphonic |
| 2-phenylaminonaph- |
| acid-amide→acetoace- |
| thalene-5-sulphonic |
| tylaminobenzene |
| acid |
| VII 2-amino-4-chloro-1- |
| 2-amino-1-hydroxy- |
| green |
| hydroxy-5-nitroben- |
| benzene-4-sulphonic |
| zine→2-phenylamino- |
| acid-methylamide ace- |
| naphthalene-4'-sul- |
| toacetylaminocyclo- |
| phonic acid hexane |
| VIII 2-amino-4,6-di- 2-amino-1-hydroxy- |
| yellow- |
| chloro-1-hydroxy- |
| benzene-4-sulphonic |
| ish |
| benzene→2-phenyl- |
| acid-2'-hydroxypro- |
| green |
| aminonaphthalene- |
| pylamide→acetoace- |
| 3'-sulphonic acid |
| tylaminobutane |
| IX 2-amino-4,6-dinitro- |
| 2-amino-1-hydroxy- |
| olive |
| 1-hydroxybenzene→2- |
| benzene-4-sulphonic |
| phenylaminonaphtha- |
| acid-3'-mehthoxypro- |
| lene-4'-sulphonic |
| pylamide→1-acetoace- |
| acid tylamino-2-chloro- |
| benzene |
| X " 2-amino-1-hydroxy- |
| olive |
| benzene-4-sulphonic |
| acid-amide→1-aceto- |
| acetylamino-2-chloro- |
| benzene |
| XI 2-amino-4,6-dinitro- |
| 2-amino-1-hydroxy- |
| olive |
| 1-hydroxybenzene→2- |
| benzene-5-sulphonic |
| phenylaminonaphtha- |
| acid-methylamide→1- |
| lene-4'-sulphonic |
| acetoacetylamino-2- |
| acid chlorobenzene |
| XII " 2-amino-1-hydroxy- |
| olive |
| benzene-5-sulphonic |
| acid methylamide→1- |
| acetoacetylamionben- |
| zene |
| XIII 2-amino-5-chloro-1- |
| " olive |
| hydroxy-4-methoxy- |
| benzene→2-phenylami- |
| nonaphthalene-6-sul- |
| phonic acid |
| XIV 2-amino-1-hydroxy- |
| 2-amino-1- olive |
| 4,6-dinitrobenzene→ |
| hydroxybenzene-4- |
| 2-phenylaminonaphtha- |
| sulphonic acid- |
| lene-4'-sulphonic |
| amide→1- |
| acid acetoacetylamino- |
| 2-methylbenzene |
| XV " 2-amino-1-hydroxy- |
| olive |
| benzene-4-sulphonic |
| acid-amide→1- |
| acetoacetylamino- |
| 2-methoxybenzene |
| XVI " 2-amino-1-hydroxy- |
| olive |
| benzene-4-sulphonic |
| acid-amide→1- |
| acetoacetylamino-2, |
| 5-dimethoxybenzene |
| ______________________________________ |
| Patent | Priority | Assignee | Title |
| 4553976, | Jan 13 1983 | CIBA-GEIGY CORPORATION, A CORP OF NEW YORK | Process for dyeing or printing polyamide fibres |
| 5123930, | Apr 27 1984 | CLARIANT FINANCE BVI LIMITED | 1:2 chromium and cobalt complexes of monoazo compounds for drying porous oxide layers on aluminum and aluminum alloy substrates |
| 5283325, | Apr 27 1984 | CLARIANT FINANCE BVI LIMITED | 1:2 chromium and cobalt complexes of monoazo compounds having further unsubstituted or substituted nitro-2-hydroxyphenyl diazo component radicals and 6- or 7-acyl-amino-1-hydroxy-3-sulfonaphthalene coupling component radicals |
| Patent | Priority | Assignee | Title |
| 3005813, | |||
| 3040019, | |||
| 3169123, | |||
| 3185676, | |||
| 3203948, | |||
| 3221003, | |||
| 3632568, | |||
| FR1,085,262, | |||
| FR1,092,850, | |||
| FR1,115,426, | |||
| FR1,431,264, | |||
| FR1,466,877, | |||
| FR1,476,587, | |||
| UK1,094,746, |
| Executed on | Assignor | Assignee | Conveyance | Frame | Reel | Doc |
| Dec 17 1974 | Sandoz Ltd. | (assignment on the face of the patent) | / |
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